Search results for "fusion"

showing 10 items of 4513 documents

Quantification of pulmonary blood flow (PBF): validation of perfusion MRI and nonlinear contrast agent (CA) dose correction with H(2)15O positron emi…

2009

Validation of quantification of pulmonary blood flow (PBF) with dynamic, contrast-enhanced MRI is still missing. A possible reason certainly lies in difficulties based on the nonlinear dependence of signal intensity (SI) from contrast agent (CA) concentration. Both aspects were addressed in this study. Nine healthy pigs were examined by first-pass perfusion MRI using gadolinium diethylenetriamine pentaacetic acid (Gd-DTPA) and HO positron emission tomography (PET) imaging. Calculations of hemodynamic parameters were based on a one-compartment model (MR) and a two-compartment model (PET). Simulations showed a significant error when assuming a linear relation between MR SI and CA dose in the …

Gadolinium DTPAPulmonary CirculationCalibration curveSwinemedia_common.quotation_subjectGadoliniumPerfusion ImagingHemodynamicschemistry.chemical_elementContrast MediaSensitivity and SpecificityStandard deviationOxygen RadioisotopesmedicineContrast (vision)AnimalsRadiology Nuclear Medicine and imagingmedia_commonmedicine.diagnostic_testbusiness.industryReproducibility of ResultsWaterMagnetic resonance imagingImage EnhancementchemistryPositron emission tomographyPositron-Emission TomographyRadiopharmaceuticalsNuclear medicinebusinessArtifactsPerfusionMagnetic Resonance AngiographyMagnetic resonance in medicine
researchProduct

Quantification of resting myocardial blood flow in a pig model of acute ischemia based on first-pass MRI

2005

Qualitative and semiquantitative contrast-enhanced (CE) dynamic perfusion MRI techniques are established as noninvasive diagnostic means of assessing coronary artery disease. However, to date quantification of myocardial blood flow (MBF) has not reached the same acceptance as MBF quantification with nuclear techniques. To validate quantification of MBF at rest using the extracellular contrast agent (CA) Gd-DTPA, we performed an animal study in a pig model of acute myocardial ischemia. We quantified MBF from MRI data with a mathematical model (MMID4) of the underlying vasculature. These MBF results were subsequently compared with the results from fluorescent microspheres. The study showed a …

Gadolinium DTPAmedicine.medical_specialtyMyocardial ischemiaSwineMyocardial IschemiaContrast MediaStatistics NonparametricAcute ischemiaCoronary artery diseaseFluorescent microspheresCoronary CirculationInternal medicinemedicineAnimalsRadiology Nuclear Medicine and imagingFirst passbusiness.industryPig modelBlood flowmedicine.diseaseMagnetic Resonance ImagingDisease Models AnimalAcute DiseaseCardiologybusinessPerfusioncirculatory and respiratory physiologyMagnetic Resonance in Medicine
researchProduct

Implementation and microbiological stability of dose-banded ganciclovir infusion bags prepared in series by a robotic system.

2018

Objectives The implementation of dose-banding (DB) in centralised, pharmacy-based cytotoxic drug preparation units allows the preparation of standardised doses in series. The aim of this study was to evaluate the feasibility of DB for the prescribing of ganciclovir (GV) infusion solutions and to investigate the microbiological stability of dose-banded, automatically prepared ready-to-administer GV infusion bags by media-fill simulation tests and sterility tests. Methods The frequency of prescription of GV doses was retrospectively analysed before and after implementing the DB scheme. Four dose-ranges or ‘bands’ and the corresponding standard doses (250, 300, 350, 400 mg) were identified. Th…

GanciclovirCytotoxic drugSterilityDrug CompoundingDrug StorageGrowth promotion030226 pharmacology & pharmacyAntiviral AgentsStandard PreparationsExtended storage03 medical and health sciences0302 clinical medicineAnimal scienceDrug StabilityRefrigerationMedicineInfusions Parenteral030212 general & internal medicineGeneral Pharmacology Toxicology and PharmaceuticsGanciclovirDrug PackagingRetrospective StudiesOriginal Researchbusiness.industryReproducibility of ResultsRoboticsRobotic systemsAseptic processingbusinessDrug ContaminationPharmacy Service Hospitalmedicine.drugEuropean journal of hospital pharmacy : science and practice
researchProduct

Studies on Holothuriapolii (echinodermata) coelomocyte lysate II. Isolation of coelomocyte hemolysins

1988

The lytic activity of the Holothuria polii coelomocyte lysate resides in two electrophoretically distinct hemolysins identified as He1 and He2. He1 represents the calcium dependent, heat-labile component whereas He2 is calcium independent and heat-stable. The two hemolysins share serological identity. Both hemolysins appear as single protein molecules of 80KDa molecular weight by SDS-PAGE and transblotting analysis under non-reducing conditions. However under reducing conditions, they are doublets of 76 and 80KDa molecular weight. The hypothesis that the two hemolysins could be isoforms is discussed.

Gel electrophoresisImmunodiffusionbiologySea CucumbersImmunologyHemolysinbiology.organism_classificationHemolysin ProteinsMicrobiologyMolecular WeightHemolysin ProteinsCytolysisRed blood cellmedicine.anatomical_structureLytic cyclemedicineAnimalsElectrophoresis Polyacrylamide GelHolothuriaCoelomocyteEchinodermataDevelopmental BiologyDevelopmental & Comparative Immunology
researchProduct

The b1 isoform of protocadherin-gamma (Pcdhgamma) interacts with the microtubule-destabilizing protein SCG10.

2004

Due to their structural characteristics and their diversity, the 22 members of the protocadherin-gamma (Pcdhgamma) family have been suggested to contribute to the establishment of specific connections in the nervous system. Here, we focus on a single isoform, Pcdhgamma-b1. Its expression is found in different brain regions and in developing spinal cord it is restricted to scattered cells, whereas all cells are labeled using an antibody that recognizes all Pcdhgamma isoforms. As a first step to understanding the signaling mechanisms downstream of Pcdhgamma, we identify the microtubule-destabilizing protein SCG10 as a cytoplasmic interactor for Pcdhgamma-b1 and other isoforms of the Pcdhgamma…

Gene isoformNervous systemSubfamilyRecombinant Fusion ProteinsBiophysicsTwo-hybridProtocadherinCadherin Related ProteinsBiologyBiochemistryMicrotubulesMiceProtocadherinStructural BiologyMicrotubuleTwo-Hybrid System TechniquesChlorocebus aethiopsGeneticsmedicineAnimalsProtein IsoformsInteractorNerve Growth FactorsGrowth coneMolecular BiologyNeuronsProtocadherin-gammaCalcium-Binding ProteinsIntracellular Signaling Peptides and ProteinsBrainCell BiologySCGIOCadherinsMolecular biologyCell biologySCG10medicine.anatomical_structureCytoplasmCOS CellsStathminGrowth coneSignal TransductionFEBS letters
researchProduct

SNAP-25a and -25b isoforms are both expressed in insulin-secreting cells and can function in insulin secretion

1999

The tSNARE (the target-membrane soluble NSF-attachment protein receptor, where NSF is N-ethylmaleimide-sensitive fusion protein) synaptosomal-associated protein of 25 kDa (SNAP-25) is expressed in pancreatic B-cells and its cleavage by botulinum neurotoxin E (BoNT/E) abolishes stimulated secretion of insulin. In the nervous system, two SNAP-25 isoforms (a and b) have been described that are produced by alternative splicing. Here it is shown, using reverse transcriptase PCR, that messages for both SNAP-25 isoforms are expressed in primary pancreatic B and non-B cells as well as in insulin-secreting cell lines. After transfection, both isoforms can be detected at the plasma membrane as well a…

Gene isoformProtein Isoforms/genetics/ metabolismBotulinum ToxinsSynaptosomal-Associated Protein 25RNA Messenger/genetics/metabolismmedicine.medical_treatmentMutantNerve Tissue ProteinsBiologyBiochemistryCell LineIslets of LangerhansInsulin SecretionmedicineBotulinum Toxins/pharmacologyInsulinProtein IsoformsAnimalsHumansSecretionRNA MessengerReceptorMolecular BiologyDNA Primersddc:616Base SequenceInsulinMembrane ProteinsCell BiologyTransfectionNerve Tissue Proteins/genetics/ metabolismFusion proteinMolecular biologyRatsCell cultureMutagenesis Site-DirectedIslets of Langerhans/cytology/drug effects/ secretionInsulin/ secretionResearch Article
researchProduct

The Xenopus Oocyte as an Ectopic Expression System for the Selection of Protein Isoform-Specific Antibodies

1993

A panel of Xenopus oocytes, each injected with cRNA coding for one specific isoform of the rat brain RCK family of voltage gated potassium channel proteins, was employed to screen for isoform-specific monoclonal antibodies. Several days after injection, cryosections of embedded oocytes were produced and were employed in immunohistochemical analysis of antibody binding. Of the advantageous properties of the assay, it employs the native antigen, it can be applied to homooligomeric and heterooligomeric proteins, and cryosections of the same batch can be stored frozen for later tests. The method may be advantageous also for the selection of isoform-specific antibodies of other protein families.

Gene isoformProtein isoformPotassium ChannelsProtein familymedicine.drug_classRecombinant Fusion ProteinsXenopusNerve Tissue ProteinsBiologyMonoclonal antibodyEpitopeMiceXenopus laevisAntigenAntibody SpecificitymedicineAnimalsPharmacologyMice Inbred BALB CHybridomasAntibodies Monoclonalbiology.organism_classificationMolecular biologyOocytesFemaleEctopic expressionJournal of Receptor Research
researchProduct

Application of an ectopic expression system for the selection of protein-isoform-specific antibodies. The monoclonal antibody K1 C3 is specific for t…

1993

Monoclonal antibodies were raised against a fusion protein consisting of a fragment of 141 amino acids of the C-terminal region of the rat brain voltage-gated K(+)-channel protein (RCK1) and the lambda N protein (fusion protein I). Selection of K(+)-channel-specific hybridoma cell lines was performed by means of an ELISA employing a fusion protein consisting of the K(+)-channel-specific peptide sequence and glutathione S-transferase (fusion protein II). For final selection of RCK1 isoform-specific antibodies, a panel of Xenopus oocytes was employed, each injected with cRNA coding for a specific RCK isoform (RCK 1, 2, 4 or 5). Several days after injection, cryosections of embedded oocytes we…

Gene isoformProtein isoformPotassium Channelsmedicine.drug_classBlotting WesternMolecular Sequence DataEnzyme-Linked Immunosorbent AssayMonoclonal antibodyBiochemistryMiceAntibody SpecificityProtein A/GTumor Cells CulturedmedicineAnimalsAmino Acid SequenceRats WistarPeptide sequenceBrain ChemistryMice Inbred BALB CHybridomasSequence Homology Amino AcidbiologyAntibodies MonoclonalFusion proteinMolecular biologyRatsBiochemistryPotassium Channels Voltage-Gatedbiology.proteinImmunohistochemistryAntibodyKv1.1 Potassium ChannelEuropean Journal of Biochemistry
researchProduct

Numerical evidence for a thermal driving force during adsorption of butane in silicalite.

2009

International audience; The transport properties of nano-porous materials determine their applicability, e.g. as separators or catalysts (J. Ka¨rger, D. Ruthven. Diffusion in zeolites, Wiley, New York (1991); L.V.C. Rees, D. Shen. Adsorption of gases in zeolite molecular sieves. In Introduction to Zeolite Science and Practice, Studies in surface science and catalysis, H.V.C. van Bekkum, E.M. Flanigen, P.A. Jacobs, J.C. Jansen (Eds.), vol. 137, pp. 579–631, Elsevier, Amsterdam (2001)). Adsorption in zeolites is explained as a two-step process; adsorption to the external crystal surface and subsequent intra-crystalline diffusion (R. M. Barrer. Porous crystal membranes. J. Chem. Soc. Faraday T…

General Chemical EngineeringDiffusion02 engineering and technology010402 general chemistryMolecular sieve01 natural sciencesIsothermal processCatalysis[PHYS.PHYS.PHYS-CHEM-PH] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]Crystalchemistry.chemical_compoundAdsorptionGeneral Materials ScienceZeoliteComputingMilieux_MISCELLANEOUSChemistryButaneGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry[CHIM.THEO] Chemical Sciences/Theoretical and/or physical chemistry[ PHYS.PHYS.PHYS-CHEM-PH ] Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]13. Climate actionModeling and SimulationPhysical Sciences[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryPhysical chemistry[PHYS.PHYS.PHYS-CHEM-PH]Physics [physics]/Physics [physics]/Chemical Physics [physics.chem-ph]0210 nano-technologyInformation Systems
researchProduct

THE GOLDMAN CONSTANT FIELD ASSUMPTION - SIGNIFICANCE AND APPLICABILITY CONDITIONS

1986

Ionic transport phenomena in simple, porous membranes can be approximately represented by the Nernst-Planck flux equations and Poisson's equation. In order to solve this set of equations for each particular case, the Goldman constant field assumption is one of the most widely used. In the present paper the significance and the applicability conditions of the above hypothesis is critically examined. and the particular situations where it is exact are shown. These conditions are later verified by solving numerically the electrodiffusion equations. The analysis carried out shows that some of the earlier studies based on asymptotic expansions and numerical solutions should be partially revised.

General Chemical EngineeringFluxConstant fieldPoisson distributionSet (abstract data type)symbols.namesakeSimple (abstract algebra)Porous membranesymbolsApplied mathematicsStatistical physicsDiffusion (business)Transport phenomenaMathematics
researchProduct